Unravelling the genetic causes of mosaic islet morphology in congenital hyperinsulinism
Abstract Congenital hyperinsulinism (CHI) causes dysregulated insulin secretion which can lead to life‐threatening hypoglycaemia if not effectively managed. CHI can be sub‐classified into three distinct groups: diffuse, focal and mosaic pancreatic disease. Whilst the underlying causes of diffuse and...
Saved in:
Main Authors: | Jayne AL Houghton (Author), Indraneel Banerjee (Author), Guftar Shaikh (Author), Shamila Jabbar (Author), Thomas W Laver (Author), Edmund Cheesman (Author), Amish Chinnoy (Author), Daphne Yau (Author), Maria Salomon‐Estebanez (Author), Mark J Dunne (Author), Sarah E Flanagan (Author) |
---|---|
Format: | Book |
Published: |
Wiley,
2020-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clustering of Hypoglycemia Events in Patients With Hyperinsulinism: Extension of the Digital Phenotype Through Retrospective Data Analysis
by: Chris Worth, et al.
Published: (2021) -
Congenital Hyperinsulinism and Evolution to Sulfonylurearesponsive Diabetes Later in Life due to a Novel Homozygous p.L171F ABCC8 Mutation
by: Emregül Işık, et al.
Published: (2019) -
Neonatal congenital hyperinsulinism in Indonesia
by: I.Made Arimbawa, et al.
Published: (2021) -
Clinical and genetic heterogeneity of congenital hyperinsulinism
by: Juncal Reguera Bernardino, et al.
Published: (2018) -
Congenital hyperinsulinism: current status and future perspectives
by: Tohru Yorifuji
Published: (2014)